Canonical Allele Identifier: PA261956
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48031
ClinVar RCV Id: RCV000041308 RCV000223811 RCV000469099 RCV000592134 RCV003236576 RCV003343619 RCV004546422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Arg377Cys
CA016641
NM_170708.4:c.1129C>T